Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP952892.RA2W-uEg8Xgmc-vBSiPgUj3x_eRMfw-RUqPTsSbz_k9Fo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP952892.RA2W-uEg8Xgmc-vBSiPgUj3x_eRMfw-RUqPTsSbz_k9Fo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP952892.RA2W-uEg8Xgmc-vBSiPgUj3x_eRMfw-RUqPTsSbz_k9Fo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP952892.RA2W-uEg8Xgmc-vBSiPgUj3x_eRMfw-RUqPTsSbz_k9Fo130_provenance.
- NP952892.RA2W-uEg8Xgmc-vBSiPgUj3x_eRMfw-RUqPTsSbz_k9Fo130_assertion description "[To elucidate the molecular mechanism of LGMD2A, we constructed nine p94 missense point mutants found in LGMD2A and analyzed their p94 unique properties.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP952892.RA2W-uEg8Xgmc-vBSiPgUj3x_eRMfw-RUqPTsSbz_k9Fo130_provenance.
- NP952892.RA2W-uEg8Xgmc-vBSiPgUj3x_eRMfw-RUqPTsSbz_k9Fo130_assertion evidence source_evidence_literature NP952892.RA2W-uEg8Xgmc-vBSiPgUj3x_eRMfw-RUqPTsSbz_k9Fo130_provenance.
- NP952892.RA2W-uEg8Xgmc-vBSiPgUj3x_eRMfw-RUqPTsSbz_k9Fo130_assertion SIO_000772 9642272 NP952892.RA2W-uEg8Xgmc-vBSiPgUj3x_eRMfw-RUqPTsSbz_k9Fo130_provenance.
- NP952892.RA2W-uEg8Xgmc-vBSiPgUj3x_eRMfw-RUqPTsSbz_k9Fo130_assertion wasDerivedFrom befree-20150227 NP952892.RA2W-uEg8Xgmc-vBSiPgUj3x_eRMfw-RUqPTsSbz_k9Fo130_provenance.
- NP952892.RA2W-uEg8Xgmc-vBSiPgUj3x_eRMfw-RUqPTsSbz_k9Fo130_assertion wasGeneratedBy ECO_0000203 NP952892.RA2W-uEg8Xgmc-vBSiPgUj3x_eRMfw-RUqPTsSbz_k9Fo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP952892.RA2W-uEg8Xgmc-vBSiPgUj3x_eRMfw-RUqPTsSbz_k9Fo130_provenance.